US827180A - Process of electrolytically removing scale and producing iron sulfate. - Google Patents
Process of electrolytically removing scale and producing iron sulfate. Download PDFInfo
- Publication number
- US827180A US827180A US29429206A US1906294292A US827180A US 827180 A US827180 A US 827180A US 29429206 A US29429206 A US 29429206A US 1906294292 A US1906294292 A US 1906294292A US 827180 A US827180 A US 827180A
- Authority
- US
- United States
- Prior art keywords
- metal
- electrolyte
- scale
- cathode
- iron
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title description 18
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 title description 10
- 229910000358 iron sulfate Inorganic materials 0.000 title description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 30
- 229910052751 metal Inorganic materials 0.000 description 28
- 239000002184 metal Substances 0.000 description 28
- 239000003792 electrolyte Substances 0.000 description 25
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 16
- 239000000243 solution Substances 0.000 description 15
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 12
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical compound [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 11
- 239000002253 acid Substances 0.000 description 8
- 239000007864 aqueous solution Substances 0.000 description 7
- 229910052742 iron Inorganic materials 0.000 description 6
- 235000003891 ferrous sulphate Nutrition 0.000 description 4
- 239000011790 ferrous sulphate Substances 0.000 description 4
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 4
- 230000001376 precipitating effect Effects 0.000 description 4
- 238000001816 cooling Methods 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 230000001788 irregular Effects 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 101100400378 Mus musculus Marveld2 gene Proteins 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- -1 alkali-metal salt Chemical class 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000001962 electrophoresis Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 235000021110 pickles Nutrition 0.000 description 1
- 239000003507 refrigerant Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25F—PROCESSES FOR THE ELECTROLYTIC REMOVAL OF MATERIALS FROM OBJECTS; APPARATUS THEREFOR
- C25F1/00—Electrolytic cleaning, degreasing, pickling or descaling
- C25F1/02—Pickling; Descaling
- C25F1/04—Pickling; Descaling in solution
- C25F1/06—Iron or steel
Definitions
- arious electrolytic methods have, been proposed for removing the oXid scale from iron sheets, rods, and wire.
- the iron article is made the anode in an electrolyte of acid or an acid salt.
- the scale is thus dissolved more rapidly than in the usual pickle bath; but the action is apt to be irregular, and solution of the iron invariably occurs.
- the gain in time is more than offset by the cost of the electric current.
- the iron article is made the cathode in an electrolyte which is neutral, weakly acid, or alkaline for exam-, ple, a dilute solution 'of an alkali-metal salt, an acid, or an alkali.
- the iron article is made the cathode in an electrolyte consistin preferably,-of a strong a neous solution if sulfuric acid.
- the scalie is thereby reduced to a lower state of oxidation and electrolytically dissolved with the production of ferrous sulfate.
- An insoluble anode is employed, and sulfur dioXid is maintained in solution in the electrolyte, serving by its oxidation to both depolarize the anode and replenish the acid in solution.
- the electrolyte consists of an aqueous solution of sulfuric acid having a specific gravity of about 1.20, equivalent to an acid content of 27.1 per cent.
- the anode may be of lead and the current density at the cathode from forty to seventy'amperes er square foot.
- the electrolyte is referab y maintained ata temerature of a out centi rade.
- the sulr dioxid may be supplie directly to the electrolytic cell, as by allowin it to .rise in bubbles along the anode, or the electrolyte may be circulated between the cell and a separate vessel, into which the gas is intro Specification of Letters Patent; Application filed January 2, 1906. Serial No. 294,292.
- a diaphragm-cell is preferably employed, the gas being supplied to the anodecompartment or anolyte to prevent its wasteful reduction to sulfur ,at the cathode. Under these conditions the reduction and solution of the scale on the cathode and the oxidation of the sulfur dioxid at the anode are 7 rapid and continuous. rate of supplyofthe gas the production of acid may be made to correspond with the rate of its consumption by the ferrous sulfate, the electrolyte thus being maintained at the proper concentration. In the case of a diaphragm-cell the concentration of the acid in the catholyte is maintained by diffusion and cataphoresis from the anolyte.
- the electrolyte. or catholyte is transferred to a shallow pan and allowed to cool. It is preferable to reduce its By regulating the temperature to about 0 centigrade by the use of a suitable refrigerant.
- the iron sulfate crystallizes out, and the residual solution is returned to the electrolytic cell, preferably to the anode-compartment, no evaporation or further treatment being required v to fit it for continued use as an electrolyte.
- I claim- 1 The process of electrolytically dissolving iron-oxid scale from the surface of metal, which consists in passing an electric current to the metal, as cathode, in an electrolyte containing sulfuric acid and sulfur dioxid, as set forth.
- the process of electrolytically dissolving iron-oxid scale from the surface of metal which. consists in interposin a diaphragm between a catholyte and ano yte containing sulfuric acid, passin an electric current .to the metal, as cathode, supplying sulfur dioxid to the anolyte, removing and cooling the catholyte, thereby precipitating the ferrous sulfate, and returning the residual solution to the anode-compartment, as set forth.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
- Electrolytic Production Of Metals (AREA)
Description
To all whom it may concern;
UNITED sTATEs PArENT OFFICE.
CHARLES J. REED, OF PHILADELPHIA, PENNSYLVANIA. PROCESS OF ELECTROLYTICALLY REMOVING SCA LE AND PRODUCING IRON SULFATE.
Be it known that I, CHARLES J. REED, a citizen of the United States, residin at Philadelphia, in the county of Philade phia and State of Pennsylvania, have invented certain new and useful Improvements in Processes of Electrolytically Removing Scale and Producing Iron Sulfate, of which the followin is a specification.
arious electrolytic methods have, been proposed for removing the oXid scale from iron sheets, rods, and wire. In some of these the iron article is made the anode in an electrolyte of acid or an acid salt. The scale is thus dissolved more rapidly than in the usual pickle bath; but the action is apt to be irregular, and solution of the iron invariably occurs. Furthermore, the gain in time is more than offset by the cost of the electric current. Inother proposed methods the iron article is made the cathode in an electrolyte which is neutral, weakly acid, or alkaline for exam-, ple, a dilute solution 'of an alkali-metal salt, an acid, or an alkali. The removal of scale, however, is slow and irregular, spots of scale being fre uentlyleft at variouspoints. Some of the sea e is also loosened by the electrolytic hydrogen and drops into the bath. In neu-' tral or alkaline solutions much of the scale is reduced to metallic iron, producing a rough irregular surface.
According to the present invention the iron article is made the cathode in an electrolyte consistin preferably,-of a strong a neous solution if sulfuric acid. The scalie is thereby reduced to a lower state of oxidation and electrolytically dissolved with the production of ferrous sulfate. An insoluble anode is employed, and sulfur dioXid is maintained in solution in the electrolyte, serving by its oxidation to both depolarize the anode and replenish the acid in solution.
In the preferred mode of procedure the electrolyte consists of an aqueous solution of sulfuric acid having a specific gravity of about 1.20, equivalent to an acid content of 27.1 per cent. The anode may be of lead and the current density at the cathode from forty to seventy'amperes er square foot. The electrolyte is referab y maintained ata temerature of a out centi rade. The sulr dioxid may be supplie directly to the electrolytic cell, as by allowin it to .rise in bubbles along the anode, or the electrolyte may be circulated between the cell and a separate vessel, into which the gas is intro Specification of Letters Patent; Application filed January 2, 1906. Serial No. 294,292.
l'atented July 31, 1906.
duced. A diaphragm-cell is preferably employed, the gas being supplied to the anodecompartment or anolyte to prevent its wasteful reduction to sulfur ,at the cathode. Under these conditions the reduction and solution of the scale on the cathode and the oxidation of the sulfur dioxid at the anode are 7 rapid and continuous. rate of supplyofthe gas the production of acid may be made to correspond with the rate of its consumption by the ferrous sulfate, the electrolyte thus being maintained at the proper concentration. In the case of a diaphragm-cell the concentration of the acid in the catholyte is maintained by diffusion and cataphoresis from the anolyte.
As the amount of iron sulfate in solution approaches saturation the electrolyte. or catholyte is transferred to a shallow pan and allowed to cool. It is preferable to reduce its By regulating the temperature to about 0 centigrade by the use of a suitable refrigerant. The iron sulfate crystallizes out, and the residual solution is returned to the electrolytic cell, preferably to the anode-compartment, no evaporation or further treatment being required v to fit it for continued use as an electrolyte.
I claim- 1. The process of electrolytically dissolving iron-oxid scale from the surface of metal, which consists in passing an electric current to the metal, as cathode, in an electrolyte containing sulfuric acid and sulfur dioxid, as set forth.
2. The process of electrolytically dissolving iron-oxid scale from the surface of metal, which consists in passing an electric current to the metal, as cathode, in an electrolyte consistin of a strong aqueous solution of sulfuric aci impregnated With sulfur dioxid, as set forth.
3. The process of electrolytically dissolving iron-oxid. scale from the surface of metal, which consists in passing to the metal as cathode, in an electrolyte consisting of 'a heated, strong aqueous solution of sulfuric acid impregnated with sulfur dioxid, an elec tric current of sufficient density to rapidly revmove the scale, as set forth.
4. The process of electrolytically dissolving iron-oxid scale from the surface of metal, which consists in passin an electric current to the metal, as catho e, in an electrolyte containing sulfuric acid, and introducing sulfur dioxid intothe electrolyte, as set forth.
5. The process of electrolytically dissolv- IIO ingiron-oxid scale from the surface of metal, which consists in passing an electric current to the metal, as cathode, in an electrolyte consisting of a strong aqueous solution of sulfuric acid, and introducing sulfur dioxid into the electrolyte, as set forth.
6. The process of electrolytically dissolving iron-oxid scale from the surface of metal, which consists in passing to the metal, as cathode, in an electrolyte consisting of a heated, strong aqueous solution of sulfuric acid, an electric current of sufficient density to rapidly remove the scale, and introducing sulfur dioXid into the electrolyte, as set forth.
7. The process of electrolytically dissolving iron-oxid scale from the surface of metal, which consists in passing an electric current to the metal, as cathode, in an electrolyte containing sulfuric acid and sulfur dioxid, and recovering the iron sulfate from the resulting solution, as set forth.
8. The process of electrolytically dissolving iron-oxid scale from the surface of metal, which consists in passing an electric current to the metal, as cathode, in an electrolyte containing sulfuric acid and sulfur dioXid, withdrawing the resulting solution, recovering the iron sulfate therein and returning the solution to the electrolytic cell, as set forth.
9. The process of electrolytically dissolving iron-oxid scale fromthe surface of metal, which. consists in passing an electric current to the metal, as cathode, in an electrolyte containing sulfuric acid and sulfur dioxid, withdrawing and cooling the resulting solution, thereby precipitating the iron sulfate, and returning the residual solution to the electrolytic cell, as set forth.
10'. The process of electrolytically dissolving iron-oxid scale from the surface of metal, which consists in interposing a diaphragm between a catholyte and anolyte containing sulfuric acid, passing an electric current to the metal, as cathode, and supplying sulfur dioxid to the anolyte, as set forth.
11. The process of electrolytically dissolving ir0n-oxid scale from the surface of metal, which consists in interposing a diaphragm between a catholyte and anolyte consisting of a strong aqueous solution of sulfuric acid, passing an electric current to the metal, as cathode, heatin the electrolyte, and supplying sulfur dioxid to the anolyte, as set forth.
12. The process of electrolytically dissolving iron-oxid scale from the surface of metal, which consists in inter )osing a diaphragm between a catholyte an anolyte containing sulfuric acid, passing an electric current to the metal, as cathode, supplying sulfur dioxid to the anolyte, and circulating the electrolyte between the cell and a precipitating vessel, as set forth.
13. The process of electrolytically dissolving iron-oxid scale from the surface of metal, which. consists in interposin a diaphragm between a catholyte and ano yte containing sulfuric acid, passin an electric current .to the metal, as cathode, supplying sulfur dioxid to the anolyte, removing and cooling the catholyte, thereby precipitating the ferrous sulfate, and returning the residual solution to the anode-compartment, as set forth.
14. The process of electrolytically dissolving iron-oX1d scale from the surface of metal, which consists in interposing a diaphragm between a catholyte and anolyte consisting of a strong aqueous solution of sulfuric acid, passing an electric current to the metal, as cathode, heating the electrolyte, supplyin sulfur dioxid to the anolyte, removing and cooling the catholyte, thereby precipitating the ferrous sulfate, and returning the residual solution to the anode-compartment, as set forth.
In testimony whereof I affix my signature in presence of two witnesses.
CHARLES J. REED. Witnesses:
JAY D. REED. M. J. REED.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US29429206A US827180A (en) | 1906-01-02 | 1906-01-02 | Process of electrolytically removing scale and producing iron sulfate. |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US29429206A US827180A (en) | 1906-01-02 | 1906-01-02 | Process of electrolytically removing scale and producing iron sulfate. |
Publications (1)
Publication Number | Publication Date |
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US827180A true US827180A (en) | 1906-07-31 |
Family
ID=2895660
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US29429206A Expired - Lifetime US827180A (en) | 1906-01-02 | 1906-01-02 | Process of electrolytically removing scale and producing iron sulfate. |
Country Status (1)
Country | Link |
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US (1) | US827180A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2448262A (en) * | 1943-07-19 | 1948-08-31 | Du Pont | Metal cleaning |
-
1906
- 1906-01-02 US US29429206A patent/US827180A/en not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2448262A (en) * | 1943-07-19 | 1948-08-31 | Du Pont | Metal cleaning |
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